Time-varying age- and CD4-stratified rates of mortality and WHO stage 3 and stage 4 events in children, adolescents and youth 0 to 24 years living with perinatally acquired HIV, before and after antiretroviral therapy initiation in the paediatric IeDEA Global Cohort Consortium.


Journal

Journal of the International AIDS Society
ISSN: 1758-2652
Titre abrégé: J Int AIDS Soc
Pays: Switzerland
ID NLM: 101478566

Informations de publication

Date de publication:
10 2020
Historique:
received: 17 02 2020
revised: 10 07 2020
accepted: 09 08 2020
entrez: 9 10 2020
pubmed: 10 10 2020
medline: 10 4 2021
Statut: ppublish

Résumé

Evaluating outcomes of paediatric patients with HIV provides crucial data for clinicians and policymakers. We analysed mortality and clinical events rates among children, adolescents, and youth with perinatally acquired HIV (PHIV) aged 0 to 24 years stratified by time-varying age and CD4, before and after antiretroviral therapy (ART), in the paediatric IeDEA multiregional collaboration (East, West, Central and Southern Africa, Asia-Pacific, and Central/South America and the Caribbean). ART-naïve children with HIV enrolled before age 10 (proxy for perinatal infection) at IeDEA sites between 2004 and 2016, with ≥1 CD4 measurement during follow-up were included. We estimated incidence rates (IR) and 95% confidence intervals (95% CI) of mortality and first occurrence of WHO-4 and WHO-3 events, excluding tuberculosis, during person-years (PY) spent within different age (<2, 2 to 4, 5 to 9, 10 to 14, 15 to 19, 20 to 24) and CD4 (percent when <5 years [<15%, 15% to 24%, ≥25%]; count when ≥5 years [<200, 200 to 499, ≥500 cells/µL]) strata. We used linear mixed models to predict CD4 evolution, with trends modelled by region. In the pre-ART period, 49 137 participants contributed 51 966 PY of follow-up (median enrolment age: 3.9 years). The overall pre-ART IRs were 2.8/100 PY (95% CI: 2.7 to 2.9) for mortality, 3.3/100 PY (95% CI: 3.0 to 3.5) for first occurrence of a WHO-4 event, and 7.0/100 PY (95% CI: 6.7 to 7.4) for first occurrence of a WHO-3 event. Lower CD4 and younger age strata were associated with increased rates of both mortality and first occurrence of a clinical event. In the post-ART period, 52 147 PHIVY contributed 207 945 PY (ART initiation median age: 4.5 years). Overall mortality IR was 1.4/100 PY (95% CI: 1.4 to 1.5) and higher in low CD4 strata; patients at each end of the age spectrum (<2 and >19) had increased mortality post-ART. IRs for first occurrence of WHO-4 and WHO-3 events were 1.3/100 PY (95% CI: 1.2 to 1.4) and 2.1/100 PY (95% CI: 2.0 to 2.2) respectively. These were also associated with lower CD4 and younger age strata. Mortality and incidence of clinical events were highest in both younger (<2 years) and older (>19 years) youth with PHIV. Scaling-up services for <2 years (early access to HIV diagnosis and care) and >19 years (adolescent- and youth-focused health services) is critical to improve outcomes among PHIVY.

Identifiants

pubmed: 33034417
doi: 10.1002/jia2.25617
pmc: PMC7545918
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e25617

Subventions

Organisme : NHLBI NIH HHS
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI096299
Pays : United States
Organisme : NIH HHS
ID : K08 HD094638
Pays : United States
Organisme : NIAAA NIH HHS
Pays : United States
Organisme : NIMH NIH HHS
Pays : United States
Organisme : NLM NIH HHS
Pays : United States
Organisme : NIH HHS
ID : U01AI069924
Pays : United States
Organisme : NIH HHS
ID : U01AI069907
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD079214
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069911
Pays : United States
Organisme : NCI NIH HHS
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069907
Pays : United States
Organisme : NIH HHS
ID : U01AI096299
Pays : United States
Organisme : FIC NIH HHS
Pays : United States
Organisme : NIH HHS
ID : U01AI069923
Pays : United States
Organisme : NIH HHS
ID : U01AI069919
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069923
Pays : United States
Organisme : NIAID NIH HHS
ID : R24 AI124872
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI027763
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069919
Pays : United States
Organisme : NIDDK NIH HHS
Pays : United States
Organisme : NIH HHS
ID : R01HD079214
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI060354
Pays : United States
Organisme : NIDA NIH HHS
Pays : United States
Organisme : NIH HHS
ID : U01AI069911
Pays : United States
Organisme : NICHD NIH HHS
ID : K08 HD094638
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069924
Pays : United States

Informations de copyright

© 2020 The Authors. Journal of the International AIDS Society published by John Wiley & Sons Ltd on behalf of the International AIDS Society.

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Auteurs

Sophie Desmonde (S)

Inserm U1027, Université Paul Sabatier Toulouse 3, Toulouse, France.

Anne M Neilan (AM)

Division of General Academic Pediatrics, Department of Pediatrics, Massachusetts General Hospital for Children, Boston, MA, USA.

Beverly Musick (B)

School of Medicine, Indiana University, Indianapolis, IN, USA.

Gabriela Patten (G)

School of Public Health and Family Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Kulkanya Chokephaibulkit (K)

Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

Andrew Edmonds (A)

Department of Epidemiology, Gillings School of Global Public Health, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Stephany N Duda (SN)

Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN, USA.

Karen Malateste (K)

Inserm U1219, Université de Bordeaux, Bordeaux, France.
Bordeaux Population Health Center, Université de Bordeaux, Bordeaux, France.

Kara Wools-Kaloustian (K)

School of Medicine, Indiana University, Indianapolis, IN, USA.

Andrea L Ciaranello (AL)

Division of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.

Mary-Ann Davies (MA)

School of Public Health and Family Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Valériane Leroy (V)

Inserm U1027, Université Paul Sabatier Toulouse 3, Toulouse, France.

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